Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Common FSNP variants of fourteen Bardet-Biedl syndrome genes and adult body mass.

Obesity (Silver Spring, Md.) - 1 Aug 2013

Birk Ruth Z, Ermakov Sergey, Livshits Gregory

Abstract excerpt

OBJECTIVE: Bardet-Biedl syndrome (BBS) is a rare monogenic multi-systemic disorder manifesting with marked obesity. Fourteen BBS genes have been identified to date and additional loci are expected. Mutations of several BBS genes were shown to affect fat cell differentiation. The purpose was to Investigate the association between common polymorphisms in all 14 genes as a group and body weight. DESIGN AND METHODS:...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Bardet-Biedl Syndrome
Share to Body Composition
Share to Body Mass Index

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Body Weight

Share to Microtubule-Associated Proteins

Share to Obesity

Share to Principal Component Analysis

Share to United Kingdom

Source

Identifiers

PMID: 23404957
DOI: 10.1002/oby.20056

Genes

BBS9

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Common FSNP variants of fourteen Bardet-Biedl syndrome genes and adult body mass.PMID 23404957Read ↗

Bardet-Biedl syndrome gene variants are associated with both childhood and adult common obesity in French Caucasians.Semantic proximity Read ↗

Weighted Burden Analysis of Rare Genetic Variants Identifies Novel Genes with Effects on BMI.Semantic proximity Read ↗

Whole Exome Sequencing in 11 Iranian Patients Expands the Mutational and Clinical Spectrum of Bardet- Biedl SyndromeSemantic proximity Read ↗

Biallelic Variants in Seven Different Genes Associated with Clinically Suspected Bardet-Biedl Syndrome.Semantic proximity Read ↗

Evaluation of complex inheritance involving the most common Bardet-Biedl syndrome locus (BBS1).Semantic proximity Read ↗

Canadian Bardet-Biedl syndrome family reduces the critical region of BBS3 (3p) and presents with a variable phenotype.Semantic proximity Read ↗

Bardet-Biedl syndrome: a molecular and phenotypic study of 18 families.Semantic proximity Read ↗

Adipose tissue function and insulin sensitivity in syndromic obesity of Bardet-Biedl SyndromeSemantic proximity Read ↗

Whole Exome Sequencing Identifies a Novel and a Recurrent Mutation in BBS2 Gene in a Family with Bardet-Biedl Syndrome.Semantic proximity Read ↗

Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome.Semantic proximity Read ↗

Delineating the Spectrum of Genetic Variants Associated with Bardet-Biedl Syndrome in Consanguineous Pakistani Pedigrees.Semantic proximity Read ↗

Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2).Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.